HuGE Literature Finder
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| Familial Mediterranean fever is associated with a wide spectrum of inflammatory disorders: results from a large cohort study. Rheumatology international 2019 Aug . Atas Nuh, Armagan Berkan, Bodakci Erdal, Satis Hasan, Sari Alper, Bilge Nazife Sule Yasar, Salman Reyhan Bilici, Yardimci Gozde Kubra, Babaoglu Hakan, Guler Aslihan Avanoglu, Karadeniz Hazan, Kilic Levent, Ozturk Mehmet Akif, Goker Berna, Haznedaroglu Seminur, Kalyoncu Umut, Kasifoglu Timucin, Tufan Abdurrahm |
| Vasculitis and long standing ankylosing spondylitis in a patient with familial Mediterranean fever. Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences 2014 Oct 19 (10): 1009-11. Taylan Ali, Yildiz Yasar, Sari Ismail, Ozkok Gul |
| MEFV gene mutations in Egyptian children with Henoch-Schonlein purpura. Pediatric rheumatology online journal 2014 12 41. Salah Samia, Rizk Samia, Lotfy Hala M, El Houchi Salma, Marzouk Huda, Farag Yom |
| The genetics of Henoch-Schönlein purpura: a systematic review and meta-analysis. Rheumatology international 2013 Jun 33 (6): 1387-95. He Xuelian, Yu Chunhua, Zhao Peiwei, Ding Yan, Liang Xiaohui, Zhao Yulan, Yue Xin, Wu Yanxiang, Yin W |
| Familial Mediterranean fever in Germany: clinical presentation and amyloidosis risk. Scandinavian journal of rheumatology 2013 42 (1): 52-8. Ebrahimi-Fakhari D, Schönland S O, Hegenbart U, Lohse P, Beimler J, Wahlster L, Ho A D, Lorenz H-M, Blank |
| Lack of association between E148Q MEFV variant and Kawasaki disease. Human immunology 2009 Jun 70 (6): 468-71. Yamaguchi Kenichiro, Ikeda Kazuyuki, Ihara Kenji, Takada Hidetoshi, Kusuhara Koichi, Hara Toshi |
| E148Q is a disease-causing MEFV mutation: a phenotypic evaluation in patients with familial Mediterranean fever. Annals of the rheumatic diseases 2005 May 64 (5): 750-2. Topaloglu R, Ozaltin F, Yilmaz E, Ozen S, Balci B, Besbas N, Bakkaloglu |
| Mutations in the gene for familial Mediterranean fever: do they predispose to inflammation? The Journal of rheumatology 2003 Sep 30 (9): 2014-8. Ozen Seza, Bakkaloglu Aysin, Yilmaz Engin, Duzova Ali, Balci Banu, Topaloglu Rezan, Besbas Nesr |
| Common FMF alleles may predispose to development of Behcet's disease with increased risk for venous thrombosis. Scandinavian journal of rheumatology 0 36 (1): 48-52. Rabinovich E, Shinar Y, Leiba M, Ehrenfeld M, Langevitz P, Livneh |
| MEFV gene mutations (M694V, V726A, M680I, and A744S) in Iranian children with Henoch-Schönlein purpura. Pneumologia (Bucharest, Romania) 0 61 (2): 84-7. Nikibakhsh Ahmad-Ali, Houshmand Mohammad, Bagheri Morteza, Zadeh Hashem Mahmood, Rad Isa Ab |
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- Page last updated:May 20, 2022
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